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Neopentyl alcohol

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(Redirected from 2,2-Dimethylpropan-1-ol)
Neopentyl alcohol
Ball-and-stick model of the neopentyl alcohol molecule
Names
Preferred IUPAC name 2,2-Dimethylpropan-1-ol
Other names tert-Butyl carbinol
tert-Butylmethanol
Neoamyl alcohol
Neopentanol
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.000.826 Edit this at Wikidata
EC Number
  • 200-907-3
PubChem CID
UNII
UN number 1325
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C5H12O/c1-5(2,3)4-6/h6H,4H2,1-3H3Key: KPSSIOMAKSHJJG-UHFFFAOYSA-N
  • InChI=1/C5H12O/c1-5(2,3)4-6/h6H,4H2,1-3H3Key: KPSSIOMAKSHJJG-UHFFFAOYAJ
SMILES
  • CC(CO)(C)C
Properties
Chemical formula C5H12O
Molar mass 88.150 g·mol
Density 0.812 g/mL at 20 °C
Melting point 52.5 °C (126.5 °F; 325.6 K)
Boiling point 113.5 °C (236.3 °F; 386.6 K)
Solubility in water 36 g/L
Solubility very soluble in ethanol, diethyl ether
Thermochemistry
Std enthalpy of
formation
fH298)
-399.4 kJ·mol
Hazards
GHS labelling:
Pictograms GHS02: FlammableGHS07: Exclamation mark
Signal word Warning
Hazard statements H226, H228, H319, H332, H335
Precautionary statements P210, P233, P240, P241, P242, P243, P261, P264+P265, P271, P280, P303+P361+P353, P304+P340, P305+P351+P338, P317, P319, P337+P317, P370+P378, P403+P233, P403+P235, P405, P501
Flash point 37 °C (99 °F; 310 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

Neopentyl alcohol is a compound with formula (CH3)3CCH2OH. It is a colorless solid. The compound is one of the eight isomers of pentyl alcohol.

Preparation and reactions

Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride. Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with sodium amalgam.

Neopentyl alcohol can be converted to neopentyl iodide by treatment with triphenylphosphite/methyl iodide:

(CH3)3CCH2OH + I → (CH3)3CCH2I + [CH3(C6H5O)2PO + C6H5OH

See also

References

  1. Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 3–228, 5–42, 8–102, 16–22, ISBN 0-8493-0594-2
  2. "Neopentyl alcohol". pubchem.ncbi.nlm.nih.gov.
  3. Joseph Hoffman (1960). "Neopentyl Alcohol". Organic Syntheses. 40: 76. doi:10.15227/orgsyn.040.0076.
  4. Comptes Rendus, 1891, 112, p. 1065
  5. H. N. Rydon (1971). "Alkyl Iodides: Neopentyl Iodide and Iodocyclohexane". Organic Syntheses. 51: 44. doi:10.15227/orgsyn.051.0044.
Alcohols
By consumption
Alcohols found in
alcoholic drinks
Medical alcohol
Toxic alcohols
Primary
alcohols
(1°)
Methanol
Ethanol
Butanol
Straight-chain
saturated
C1 — C9
Straight-chain
saturated
C10 — C19
Straight-chain
saturated
C20 — C29
Straight-chain
saturated
C30 — C39
Straight-chain
saturated
C40 — C49
Secondary
alcohols (2°)
  • 1-Phenylethanol
  • 2-Butanol
  • 2-Deoxyerythritol
  • 2-Heptanol
  • 3-Heptanol
  • 2-Hexanol
  • 3-Hexanol
  • 3-Methyl-2-butanol
  • 2-Nonanol
  • 2-Octanol
  • 2-Pentanol
  • 3-Pentanol
  • Cyclohexanol
  • Cyclopentanol
  • Cyclopropanol
  • Diphenylmethanol
  • Isopropanol
  • Pinacolyl alcohol
  • Pirkle's alcohol
  • Propylene glycol methyl ether
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